GENEOSCOPY INC

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3026996410

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3026996410
FEI Number
3026996410
Entity Name
GENEOSCOPY INC
City/State/Country
Saint Louis, MO, US
Establishment Address
2220 Welsch Industrial Ct, Saint Louis, MO 63146, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Geneoscopy Inc (Owner Number: 10085052)
Owner / Operator Contact Address
2220 Welsch Industrial Ct, Saint Louis, MO 63146, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P230001

All Registered Proprietary Names

ColoSense

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SBB System, Colorectal Neoplasia, Rna Markers And Hemoglobin Detection Unknown Class 3 N/A 2024-05-06

Official Correspondent

Mindy Rushing

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Geneoscopy Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026996410. Last updated year: 2026. Please use registration number 3026996410 when referencing this establishment in official correspondence.
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